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International Ophthalmology|January 17, 2012
Glaucoma therapy escalation in eyes with pseudophakic corneal edema after penetrating keratoplasty and Descemet's stripping automated endothelial keratoplastyGeorge R Wandling, Matthew P Rauen, Kenneth M Goins, et al.Journal of Glaucoma|April 18, 2007
Diurnal fluctuation and concordance of intraocular pressure in glaucoma suspects and normal tension glaucoma patientsLesya M Shuba, Andrew P Doan, Michael K Maley, et al.Nature Genetics|June 10, 1998
A novel homeobox gene PITX3 is mutated in families with autosomal-dominant cataracts and ASMDE V Semina, R E Ferrell, H A Mintz-Hittner, et al.Human Molecular Genetics|August 1, 1995
Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25)E Héon, B P Sheth, J W Kalenak, et al.Nature Genetics|September 1, 1992
Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4J C Murray, S R Bennett, A E Kwitek, et al.Experimental Eye Research|May 9, 2006
Retinal synthesis and deposition of complement components induced by ocular hypertensionMarkus H Kuehn, Chan Y Kim, Jelena Ostojic, et al.Survey of Ophthalmology|November 18, 2017
Glaucoma-associated corneal endothelial cell damage: A reviewBen J Janson, Wallace L Alward, Young H Kwon, et al.American Journal of Ophthalmology|March 5, 2003
A family with Axenfeld-Rieger syndrome and Peters Anomaly caused by a point mutation (Phe112Ser) in the FOXC1 geneRobert A Honkanen, Darryl Y Nishimura, Ruth E Swiderski, et al.Developmental Dynamics : an Official Publication of the American Association of Anatomists|September 4, 1999
Expression of the Mf1 gene in developing mouse hearts: implication in the development of human congenital heart defectsR E Swiderski, R S Reiter, D Y Nishimura, et al.Journal of Glaucoma|October 7, 2017
Genomic Organization of TBK1 Copy Number Variations in Glaucoma PatientsAdam P DeLuca, Wallace L M Alward, Jeffrey Liebmann, et al.Pageof 23